Chestal Cough and Mucus Tablets
- Manufacturer
- Boiron | Boiron, Inc.
- Effective date
- 2026-03-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:38:08
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients** (in each tablet)
Antimonium tartaricum 6C HPUS (0.28 mg) (contains less than 10 -12 mg antimony)
Bryonia 3C HPUS (0.28 mg)
Coccus cacti 3C HPUS (0.28 mg)
Drosera 3C HPUS (0.28 mg)
Ipecacuanha 3C HPUS (0.28 mg) (contains less than 10 -8 mg emetine alkaloids)
Pulsatilla 6C HPUS (0.28 mg)
Rumex crispus 6C HPUS (0.28 mg) (contains less than 10 -15 mg anthraquinone glycosides)
Spongia tosta 3C HPUS (0.28 mg)
Sticta pulmonaria 3C HPUS (0.28 mg)
The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
OTC - PURPOSE SECTION
Purpose*
Antimonium tartaricum 6C HPUS (0.28 mg)………..……Helps loosen thick mucus
Bryonia 3C HPUS (0.28 mg)……..…………..……………Relieves dry and painful cough
Coccus cacti 3C HPUS (0.28 mg)……..Relieves cough associated with a tickling in the throat
Drosera 3C HPUS (0.28 mg)………….…………Relieves barking cough worse at night
Ipecacuanha 3C HPUS (0.28 mg)……………Relieves cough associated with nausea
Pulsatilla 6C HPUS (0.28 mg)……Relieves wet cough during the day becoming dry at night
Rumex crispus 6C HPUS (0.28 mg)…………Relieves dry cough triggered by cold air
Spongia tosta 3C HPUS (0.28 mg)……….… Relieves dry, croupy, and barking cough
Sticta pulmonaria 3C HPUS (0.28 mg)……………. Relieves nighttime hacking cough
INDICATIONS & USAGE SECTION
Uses*
▪ temporarily relieves dry cough due to minor throat and bronchial irritation as may occur with a cold
▪ helps relieve chest congestion due to common colds by loosening mucus and thinning bronchial secretions to make coughs more productive
WARNINGS SECTION
Do not use if you are allergic to any of this product's ingredients.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
▪ cough that occurs with too much phlegm (mucus)
▪ cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema
OTC - STOP USE SECTION
Stop use and ask a doctor if cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or a persistent headache. These could be signs of a serious condition.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Adults and children 6 years of age and older At the onset of symptoms, dissolve 2 tablets in the mouth every hour. Decrease frequency with improvement.
Children 4 to under 6 years of age Dissolve 2 tablets in 1 tablespoon of water for easier intake. Follow directions above.
Children under 4 years of age Ask a doctor.
INACTIVE INGREDIENT SECTION
croscarmellose sodium, lactose, magnesium stearate
OTC - QUESTIONS SECTION
BoironUSA.com
Info@Boiron.com
1-800-BOIRON-1 (1-800-264-7661)
SPL UNCLASSIFIED SECTION
▪ do not use if glued carton end flaps are open or if the blister seal is broken
▪ store below 86°F (30°C)
▪ retain carton for full drug facts
Made in France
Distributed by Boiron Inc.
Newtown Square, PA 19073
COUGH & MUCUS RELIEF*
Chest Congestion
Dry, Fitful Cough*
- Day & Night Multi-Symptom Relief
- Non-Drowsy
60 MELTAWAY TABLETS
Unflavored
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C, K, CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-9115-04 | CHESTAL COUGH AND MUCUS | 20 in 1 BLISTER PACK | TABLET | 20 | 1 | |
| 0220-9115-04 | CHESTAL COUGH AND MUCUS | 3 in 1 CARTON | TABLET | 3 | 1 |
Products#
Every source-derived product name is available through these pages.
- CHESTAL COUGH AND MUCUS
- ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA
- SPONGIA OFFICINALIS SKELETON, ROASTED
- MAGNESIUM STEARATE
- IPECAC
- CROSCARMELLOSE SODIUM
- RUMEX CRISPUS ROOT
- LOBARIA PULMONARIA
- PROTORTONIA CACTI
- DROSERA ROTUNDIFOLIA
- LACTOSE
- PULSATILLA VULGARIS WHOLE
- ANTIMONY POTASSIUM TARTRATE
- ANTIMONY CATION (3+)
- BRYONIA ALBA ROOT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-9115 | 0220-9115-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SPONGIA OFFICINALIS SKELETON, ROASTED | 1PIP394IID | ACTIB |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| IPECAC | 62I3C8233L | ACTIB |
| CROSCARMELLOSE SODIUM | M28OL1HH48 | IACT |
| RUMEX CRISPUS ROOT | 9N1RM2S62C | ACTIB |
| LOBARIA PULMONARIA | D1YM0P5Z2T | ACTIB |
| PROTORTONIA CACTI | LZB7TFX1LT | ACTIB |
| DROSERA ROTUNDIFOLIA | QR44N9XPJQ | ACTIB |
| LACTOSE | J2B2A4N98G | IACT |
| PULSATILLA VULGARIS WHOLE | I76KB35JEV | ACTIB |
| ANTIMONY POTASSIUM TARTRATE | DL6OZ476V3 | ACTIB |
| BRYONIA ALBA ROOT | T7J046YI2B | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| CHESTAL COUGH AND MUCUS | ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA | Boiron | 4d77a058-e6c8-2af5-e063-6394a90afe1a | 2026-03-20 | Warnings | 0220-9115-04 0220-9115 00220911504 4d77a058-e6c9-2af5-e063-6394a90afe1a 4d77a058-e6c8-2af5-e063-6394a90afe1a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

